» Articles » PMID: 38240400

Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit

Overview
Journal Ethics Hum Res
Specialty Medical Ethics
Date 2024 Jan 19
PMID 38240400
Authors
Affiliations
Soon will be listed here.
Abstract

Translational research has tended to ignore the question of whether receiving a genomic diagnosis provides utility in community care contexts outside of doctors' offices and hospitals. However, empirical research with parents has highlighted numerous ways that a genomic diagnosis might be of practical value in the care provided by teachers, physical or occupational therapists, speech-language pathologists, behavior analysts, and nonphysician mental health providers. In this essay, we propose a new conceptual model of genomic utility that offers the opportunity to better capture a broad range of potential implications of genomic technologies for families in various social and organizational systems. We explore crucial research directions to better understand how redefined utility might affect families and nonphysician professionals.

Citing Articles

Early Intervention services in the era of genomic medicine: setting a research agenda.

MacDuffie K, Cohn B, Appelbaum P, Brothers K, Doherty D, Goldenberg A Pediatr Res. 2024; .

PMID: 39438712 DOI: 10.1038/s41390-024-03668-5.

References
1.
Brosco J . Whose Odyssey Is It? Family-Centered Care in the Genomic Era. Hastings Cent Rep. 2018; 48 Suppl 2:S20-S22. DOI: 10.1002/hast.879. View

2.
Grosse S, Khoury M . What is the clinical utility of genetic testing?. Genet Med. 2006; 8(7):448-50. DOI: 10.1097/01.gim.0000227935.26763.c6. View

3.
Kohler J, Turbitt E, Biesecker B . Personal utility in genomic testing: a systematic literature review. Eur J Hum Genet. 2017; 25(6):662-668. PMC: 5477355. DOI: 10.1038/ejhg.2017.10. View

4.
Burke W, Atkins D, Gwinn M, Guttmacher A, Haddow J, Lau J . Genetic test evaluation: information needs of clinicians, policy makers, and the public. Am J Epidemiol. 2002; 156(4):311-8. DOI: 10.1093/aje/kwf055. View

5.
Nicholl H, Tracey C, Begley T, King C, Lynch A . Internet Use by Parents of Children With Rare Conditions: Findings From a Study on Parents' Web Information Needs. J Med Internet Res. 2017; 19(2):e51. PMC: 5350458. DOI: 10.2196/jmir.5834. View